农杆菌碱基编辑技术的建立与recA基因精准编辑型菌株应用 |
| 孙梦琳, 符晓, 祁显涛, 刘昌林, 谢传晓, 郭晋杰, 朱金洁 |
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Establishment of Base Editing Technology in Agrobacterium and Application of recA Gene Precisely Edited Strains |
| Sun Menglin, Fu Xiao, Qi Xiantao, Liu Changlin, Xie Chuanxiao, Guo Jinjie, Zhu Jinjie |
| 图4 基于EHA105(ΔrecA)菌株的三元载体系统对玉米幼胚的瞬时侵染 (a) pVS1或pRiA4复制子辅助质粒载体结构示意图;(b) 表达报告基因的双元载体p3301-GUS和p3301-CRC的结构示意图;(c) 基于EHA105(ΔrecA)菌株的三元载体系统对玉米幼胚的瞬时侵染;(d) 基于EHA105(ΔrecA)菌株的三元系统侵染效率(n=18);“****”表示差异极显著(P < 0.0001)。 |
| Fig.4 Transient infection of maize immature embryos using the ternary vector system based on the EHA105(ΔrecA) strain (a) schematic diagram of helper plasmid vector structures; (b) schematic diagram of reporter binary vectors; (c) transient infection of maize immature embryos using the ternary vector system based on the EHA105(ΔrecA) strain; (d) ternary systemic infection efficiency based on EHA105(ΔrecA) strain (n=18),“****”indicates extremely significant differences (P < 0.0001). |
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